[Federal Register Volume 63, Number 29 (Thursday, February 12, 1998)] [Notices] [Page 7182] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 98-3610] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Application Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that Roche Diagnostic Systems, Inc., 1080 U.S. Highway 202, Somerville, New Jersey 08876-3771, made application to the Drug Enforcement Administration (DEA) by letter dated December 17, 1997, for registration as a bulk manufacturer of ecgonine (9180), a basic class of controlled substance listed in Schedule II. The firm plans to manufacture small quantities of ecgonine which will be further converted into derivatives for incorporation in drug of abuse detection kits. Any other such applicant and any person who is presently registered with DEA to manufacture such substance may file comments or objections to the issuance of the proposed registration. Any such comments or objections may be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, United States Department of Justice, Washington, DC 20537, Attention: DEA Federal Register Representative (CCR), and must be filed no later than April 13, 1998. Dated: January 21, 1998. John H. King, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 98-3610 Filed 2-11-98; 8:45 am] BILLING CODE 4410-09-M